A Study of the Effectiveness and Safety of AMG 386 and Sorafenib to Treat Advanced or Inoperable Hepatocellular Cancer

PHASE2CompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

August 31, 2009

Primary Completion Date

October 31, 2011

Study Completion Date

June 30, 2015

Conditions
Advanced Hepatocellular CarcinomaInoperable Hepatocellular Carcinoma
Interventions
DRUG

AMG 386

Two doses of AMG 386 (15 mg/kg) IV QW will be studied

DRUG

AMG 386

Two doses of AMG 386 (10 mg/kg) IV QW will be studied

DRUG

Sorafenib

Sorafenib 400 mg PO BID orally twice daily in an every 4 week dosing schedule for 15mg/kg cohort \& 10mg/kg cohort

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Amgen

INDUSTRY